JPH07505663A - 重合体および重合体を含有する洗剤組成物 - Google Patents

重合体および重合体を含有する洗剤組成物

Info

Publication number: JPH07505663A
Authority: JP; Japan
Prior art keywords: formula; group; polymer according; polymer; units
Prior art date: 1992-04-09
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP5518092A

Other languages

English (en)

Japanese (ja)

Inventor

ヘイルズ，ステイーブン・ジヨージ

コーシユデル，エザツト

ポライカ，ロバート

Original Assignee

ユニリーバー・ナームローゼ・ベンノートシヤープ

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1992-04-09

Filing date

1993-04-07

Publication date

1995-06-22

1993-04-07 Application filed by ユニリーバー・ナームローゼ・ベンノートシヤープ filed Critical ユニリーバー・ナームローゼ・ベンノートシヤープ

1995-06-22 Publication of JPH07505663A publication Critical patent/JPH07505663A/ja

Status Pending legal-status Critical Current

Links

229920000642 polymer Polymers 0.000 title claims description 65
239000003599 detergent Substances 0.000 title claims description 43
239000000203 mixture Substances 0.000 title claims description 34
150000001875 compounds Chemical class 0.000 claims description 26
238000000034 method Methods 0.000 claims description 18
239000000126 substance Substances 0.000 claims description 11
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
150000003254 radicals Chemical class 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 7
239000003999 initiator Substances 0.000 claims description 6
125000006850 spacer group Chemical group 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 5
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
150000008064 anhydrides Chemical class 0.000 claims description 3
238000004581 coalescence Methods 0.000 claims description 2
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
229910052751 metal Inorganic materials 0.000 claims description 2
239000002184 metal Substances 0.000 claims description 2
150000002739 metals Chemical class 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
150000001768 cations Chemical class 0.000 claims 1
230000003381 solubilizing effect Effects 0.000 claims 1
-1 maleate salt Chemical class 0.000 description 19
125000000468 ketone group Chemical group 0.000 description 17
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 14
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 13
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 12
239000002253 acid Substances 0.000 description 12
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 12
229920001897 terpolymer Polymers 0.000 description 11
102000005701 Calcium-Binding Proteins Human genes 0.000 description 10
108010045403 Calcium-Binding Proteins Proteins 0.000 description 10
238000005227 gel permeation chromatography Methods 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 9
239000000344 soap Substances 0.000 description 9
238000012360 testing method Methods 0.000 description 9
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
238000004140 cleaning Methods 0.000 description 8
150000002576 ketones Chemical class 0.000 description 8
239000011976 maleic acid Substances 0.000 description 8
239000000178 monomer Substances 0.000 description 8
238000006116 polymerization reaction Methods 0.000 description 8
239000000463 material Substances 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
238000006065 biodegradation reaction Methods 0.000 description 6
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 6
239000000047 product Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 5
239000012965 benzophenone Substances 0.000 description 5
239000007844 bleaching agent Substances 0.000 description 5
229910052799 carbon Inorganic materials 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000011734 sodium Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000004753 textile Substances 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 4
XLYOFNOQVPJJNP-ZSJDYOACSA-N Heavy water Chemical compound [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 4
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
239000012190 activator Substances 0.000 description 4
150000007942 carboxylates Chemical group 0.000 description 4
238000012512 characterization method Methods 0.000 description 4
229920005646 polycarboxylate Polymers 0.000 description 4
239000002002 slurry Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
238000005406 washing Methods 0.000 description 4
LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
238000002835 absorbance Methods 0.000 description 3
150000001252 acrylic acid derivatives Chemical class 0.000 description 3
238000012662 bulk polymerization Methods 0.000 description 3
238000007334 copolymerization reaction Methods 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 3
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000002243 precursor Substances 0.000 description 3
238000000746 purification Methods 0.000 description 3
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 2
SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 2
HEGVDGCMADQJRS-UHFFFAOYSA-N 4-methylidene-2,2-diphenyl-1,3-dioxolane Chemical compound O1C(=C)COC1(C=1C=CC=CC=1)C1=CC=CC=C1 HEGVDGCMADQJRS-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
101150020891 PRKCA gene Proteins 0.000 description 2
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
229910000323 aluminium silicate Inorganic materials 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
238000010533 azeotropic distillation Methods 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000004061 bleaching Methods 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000012467 final product Substances 0.000 description 2
239000000499 gel Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
230000036571 hydration Effects 0.000 description 2
238000006703 hydration reaction Methods 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
239000007788 liquid Substances 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
238000010992 reflux Methods 0.000 description 2
238000007142 ring opening reaction Methods 0.000 description 2
239000000523 sample Substances 0.000 description 2
150000003333 secondary alcohols Chemical class 0.000 description 2
229910001415 sodium ion Inorganic materials 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
235000019832 sodium triphosphate Nutrition 0.000 description 2
238000003756 stirring Methods 0.000 description 2
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
ZLYYJUJDFKGVKB-UPHRSURJSA-N (z)-but-2-enedioyl dichloride Chemical compound ClC(=O)\C=C/C(Cl)=O ZLYYJUJDFKGVKB-UPHRSURJSA-N 0.000 description 1
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 description 1
DSCFFEYYQKSRSV-UHFFFAOYSA-N 1L-O1-methyl-muco-inositol Natural products COC1C(O)C(O)C(O)C(O)C1O DSCFFEYYQKSRSV-UHFFFAOYSA-N 0.000 description 1
CFPOJWPDQWJEMO-UHFFFAOYSA-N 2-(1,2-dicarboxyethoxy)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)OC(C(O)=O)CC(O)=O CFPOJWPDQWJEMO-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical group FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
LVVZBNKWTVZSIU-UHFFFAOYSA-N 2-(carboxymethoxy)propanedioic acid Chemical compound OC(=O)COC(C(O)=O)C(O)=O LVVZBNKWTVZSIU-UHFFFAOYSA-N 0.000 description 1
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
OQANCOWYULDETR-UHFFFAOYSA-N 2-chlorohex-1-ene Chemical compound CCCCC(Cl)=C OQANCOWYULDETR-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
UMEHTUCYIDSLRJ-UHFFFAOYSA-N 4-methylidene-1,3-dioxolane Chemical compound C=C1COCO1 UMEHTUCYIDSLRJ-UHFFFAOYSA-N 0.000 description 1
KMVPXBDOWDXXEN-UHFFFAOYSA-N 4-nitrophenylhydrazine Chemical compound NNC1=CC=C([N+]([O-])=O)C=C1 KMVPXBDOWDXXEN-UHFFFAOYSA-N 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
235000018185 Betula X alpestris Nutrition 0.000 description 1
235000018212 Betula X uliginosa Nutrition 0.000 description 1
WJSLZXMQHNTOBA-UHFFFAOYSA-N C(CCC(=O)O)(=O)O.C(CCC(=O)O)(=O)O.C(CCC(=O)O)(=O)O.OCC(O)CO Chemical compound C(CCC(=O)O)(=O)O.C(CCC(=O)O)(=O)O.C(CCC(=O)O)(=O)O.OCC(O)CO WJSLZXMQHNTOBA-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
238000001157 Fourier transform infrared spectrum Methods 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
229930194542 Keto Natural products 0.000 description 1
AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
POYABDXOHSJEOQ-UHFFFAOYSA-N OCC(O)CO.C(CC(O)(C(=O)O)CC(=O)O)(=O)O.C(CCC(=O)O)(=O)O Chemical compound OCC(O)CO.C(CC(O)(C(=O)O)CC(=O)O)(=O)O.C(CCC(=O)O)(=O)O POYABDXOHSJEOQ-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
CPZRYQJPVUJHOS-UHFFFAOYSA-N [2-(2-phenylethyl)phenyl]methanol Chemical compound OCC1=CC=CC=C1CCC1=CC=CC=C1 CPZRYQJPVUJHOS-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
229920006243 acrylic copolymer Polymers 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
238000013459 approach Methods 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
235000021028 berry Nutrition 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
229920002988 biodegradable polymer Polymers 0.000 description 1
239000004621 biodegradable polymer Substances 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
239000004566 building material Substances 0.000 description 1
WQZQEUCNSUNRRW-UHFFFAOYSA-N butanedioic acid propane-1,2,3-triol Chemical compound OCC(O)CO.OC(=O)CCC(O)=O.OC(=O)CCC(O)=O WQZQEUCNSUNRRW-UHFFFAOYSA-N 0.000 description 1
CMFFZBGFNICZIS-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O CMFFZBGFNICZIS-UHFFFAOYSA-N 0.000 description 1
HXDRSFFFXJISME-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O HXDRSFFFXJISME-UHFFFAOYSA-N 0.000 description 1
RXKUYBRRTKRGME-UHFFFAOYSA-N butanimidamide Chemical compound CCCC(N)=N RXKUYBRRTKRGME-UHFFFAOYSA-N 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229910001424 calcium ion Inorganic materials 0.000 description 1
150000001721 carbon Chemical class 0.000 description 1
229910002091 carbon monoxide Inorganic materials 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000012297 crystallization seed Substances 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000010586 diagram Methods 0.000 description 1
238000000502 dialysis Methods 0.000 description 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 1
VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
239000003623 enhancer Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
RWLDAJMGAVDXSH-UHFFFAOYSA-N ethane-1,1,2-tricarboxylic acid Chemical compound OC(=O)CC(C(O)=O)C(O)=O RWLDAJMGAVDXSH-UHFFFAOYSA-N 0.000 description 1
229940071106 ethylenediaminetetraacetate Drugs 0.000 description 1
239000007850 fluorescent dye Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
238000010528 free radical solution polymerization reaction Methods 0.000 description 1
HZGSQPAPBIIIDM-UHFFFAOYSA-N furan-2,5-dione hydrate Chemical compound O.C1(C=C/C(=O)O1)=O HZGSQPAPBIIIDM-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
229940050410 gluconate Drugs 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
229910052816 inorganic phosphate Inorganic materials 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
150000008040 ionic compounds Chemical class 0.000 description 1
239000013627 low molecular weight specie Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000012528 membrane Substances 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
239000012457 nonaqueous media Substances 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
150000004967 organic peroxy acids Chemical class 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
238000006303 photolysis reaction Methods 0.000 description 1
230000015843 photosynthesis, light reaction Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001470 polyketone Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
FQLQNUZHYYPPBT-UHFFFAOYSA-N potassium;azane Chemical compound N.[K+] FQLQNUZHYYPPBT-UHFFFAOYSA-N 0.000 description 1
BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
230000001953 sensory effect Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
229940045872 sodium percarbonate Drugs 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
210000002784 stomach Anatomy 0.000 description 1
239000010902 straw Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000003890 succinate salts Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
JREYOWJEWZVAOR-UHFFFAOYSA-N triazanium;[3-methylbut-3-enoxy(oxido)phosphoryl] phosphate Chemical compound [NH4+].[NH4+].[NH4+].CC(=C)CCOP([O-])(=O)OP([O-])([O-])=O JREYOWJEWZVAOR-UHFFFAOYSA-N 0.000 description 1
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
238000000108 ultra-filtration Methods 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Detergent Compositions (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)

JP5518092A 1992-04-09 1993-04-07 重合体および重合体を含有する洗剤組成物 Pending JPH07505663A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB9207795.7		1992-04-09
GB929207795A GB9207795D0 (en)	1992-04-09	1992-04-09	Polymers and detergent compositions containing them
PCT/GB1993/000730 WO1993021243A1 (en)	1992-04-09	1993-04-07	Polymers and detergent compositions containing them

Publications (1)

Publication Number	Publication Date
JPH07505663A true JPH07505663A (ja)	1995-06-22

Family

ID=10713734

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP5518092A Pending JPH07505663A (ja)	1992-04-09	1993-04-07	重合体および重合体を含有する洗剤組成物

Country Status (13)

Country	Link
US (2)	US5439997A (cs)
EP (1)	EP0635033B1 (cs)
JP (1)	JPH07505663A (cs)
BR (1)	BR9306218A (cs)
CA (1)	CA2133202A1 (cs)
CZ (1)	CZ247594A3 (cs)
DE (1)	DE69305983T2 (cs)
ES (1)	ES2096914T3 (cs)
GB (1)	GB9207795D0 (cs)
HU (1)	HUT70687A (cs)
SK (1)	SK120194A3 (cs)
WO (1)	WO1993021243A1 (cs)
ZA (1)	ZA932548B (cs)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH09324018A (ja) *	1996-04-04	1997-12-16	Idemitsu Kosan Co Ltd	アクリル系重合体、その製造方法、生分解性ビルダー、洗剤組成物及び分散剤
DE19646782C2 (de) *	1996-11-13	2000-05-25	Merck Patent Gmbh	Bioresorbierbare Polymerisationsprodukte aus strahlungshärtbaren Bindemittelsystemen
US6133356A (en)	1996-12-23	2000-10-17	Shell Oil Company	Graft copolymerized compositions
DE69911020T2 (de) *	1999-10-06	2004-07-08	Dainippon Ink And Chemicals, Inc.	4-Methylen-1,3-dioxolane mit funktionellen Gruppen
US8822954B2 (en)	2008-10-23	2014-09-02	Intematix Corporation	Phosphor based authentication system

Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2382640A (en) *	1943-09-08	1945-08-14	Eastman Kodak Co	Resinous polymer of methylene dioxolane
JPS63277213A (ja) *	1987-05-08	1988-11-15	Nippon Petrochem Co Ltd	新規なエチレン共重合体

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US2445733A (en) *	1945-07-21	1948-07-20	Firestone Tire & Rubber Co	Resins from methylene dioxolanes
GB695633A (en) *	1950-04-24	1953-08-12	Ici Ltd	Polymers, including copolymers, from new esters of acrylic or methacrylic acid
US3764586A (en) *	1970-05-01	1973-10-09	C Lancelot	Polyelectrolyte builder and detergent compositions
GB1430085A (en) *	1972-04-07	1976-03-31	Fuillet J E	Polymer blends
NL159413B (nl) *	1973-01-16	1979-02-15	Ruhrchemie Ag	Werkwijze ter bereiding van afbreekbare tercopolymeren uit etheen, koolmonoxide en vinylacetaat.
US4144226A (en) *	1977-08-22	1979-03-13	Monsanto Company	Polymeric acetal carboxylates
US4169934A (en) *	1978-04-03	1979-10-02	Monsanto Company	Copolymers of keto dicarboxylates
US4219437A (en) *	1979-02-02	1980-08-26	Monsanto Company	Copolymers of keto dicarboxylates
JPS58204008A (ja) *	1982-05-24	1983-11-28	Hitachi Ltd	感光性樹脂組成物
JPS63218732A (ja) *	1987-03-06	1988-09-12	Mitsubishi Petrochem Co Ltd	共重合体
DE3714732C3 (de) *	1987-05-02	1994-07-14	Grillo Werke Ag	Copolymerisate auf der Basis von ungesättigten Carbonsäuren und zur Enolatbildung befähigten Monosacchariden, Verfahren zur Herstellung derselben und ihre Verwendung
JPS63284296A (ja) *	1987-05-15	1988-11-21	Mitsubishi Petrochem Co Ltd	洗剤組成物
US4847005A (en) *	1987-10-22	1989-07-11	Monsanto Company	Solutions of hydrolytically stable polymeric acetal carboxylate salts and stable liquid detergent compositions containing such salts
US4923941A (en) *	1987-10-28	1990-05-08	American Cyanamid Company	Carboxy-functional polymers and their use as detergent additives
US4959409A (en) *	1988-01-14	1990-09-25	The Procter & Gamble Company	Amino-functional compounds as builder/dispersants in detergent compositions
GB8813978D0 (en) *	1988-06-13	1988-07-20	Unilever Plc	Liquid detergents
JPH0224320A (ja) *	1988-07-12	1990-01-26	Mitsubishi Petrochem Co Ltd	易分解性高分子の製造法
JPH0273811A (ja) *	1988-09-08	1990-03-13	Hitachi Chem Co Ltd	アクリル酸塩−シクロヘキセノン共重合体、その中間体、それらの製造法、ビルダー及び洗浄剤組成物
JPH02294397A (ja) *	1989-05-08	1990-12-05	Mitsubishi Petrochem Co Ltd	洗剤組成物
GB8928318D0 (en) *	1989-12-14	1990-02-21	Unilever Plc	Polycarboxylate compounds and detergent compositions containing them

1992
- 1992-04-09 GB GB929207795A patent/GB9207795D0/en active Pending
1993
- 1993-04-07 SK SK1201-94A patent/SK120194A3/sk unknown
- 1993-04-07 WO PCT/GB1993/000730 patent/WO1993021243A1/en not_active Ceased
- 1993-04-07 EP EP93909039A patent/EP0635033B1/en not_active Expired - Lifetime
- 1993-04-07 ES ES93909039T patent/ES2096914T3/es not_active Expired - Lifetime
- 1993-04-07 JP JP5518092A patent/JPH07505663A/ja active Pending
- 1993-04-07 BR BR9306218A patent/BR9306218A/pt not_active Application Discontinuation
- 1993-04-07 DE DE69305983T patent/DE69305983T2/de not_active Expired - Fee Related
- 1993-04-07 HU HU9402908A patent/HUT70687A/hu unknown
- 1993-04-07 US US08/044,523 patent/US5439997A/en not_active Expired - Fee Related
- 1993-04-07 CA CA002133202A patent/CA2133202A1/en not_active Abandoned
- 1993-04-08 ZA ZA932548A patent/ZA932548B/xx unknown
1994
- 1994-10-07 CZ CZ942475A patent/CZ247594A3/cs unknown
1995
- 1995-01-04 US US08/368,530 patent/US5464558A/en not_active Expired - Fee Related

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2382640A (en) *	1943-09-08	1945-08-14	Eastman Kodak Co	Resinous polymer of methylene dioxolane
JPS63277213A (ja) *	1987-05-08	1988-11-15	Nippon Petrochem Co Ltd	新規なエチレン共重合体

Also Published As

Publication number	Publication date
US5464558A (en)	1995-11-07
ZA932548B (en)	1994-10-08
DE69305983D1 (de)	1996-12-19
BR9306218A (pt)	1998-06-23
HUT70687A (en)	1995-10-30
HU9402908D0 (en)	1995-02-28
WO1993021243A1 (en)	1993-10-28
CZ247594A3 (en)	1995-04-12
ES2096914T3 (es)	1997-03-16
DE69305983T2 (de)	1997-04-10
SK120194A3 (en)	1995-04-12
CA2133202A1 (en)	1993-10-28
GB9207795D0 (en)	1992-05-27
EP0635033B1 (en)	1996-11-13
US5439997A (en)	1995-08-08
EP0635033A1 (en)	1995-01-25

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EP0697422B1 (en)	1999-08-18	Method for preparing a polymer by solution polymerisation
EP0123108B1 (en)	1988-08-03	Maleic acid copolymer, production thereof and scale-preventing agent containing the same
EP0441022A2 (en)	1991-08-14	Low molecular weight, water-soluble copolymers, process for their preparation, and detergent compositions comprising such copolymers
JPH08508022A (ja)	1996-08-27	ペルオキシ酸
NZ241462A (en)	1994-02-25	Terpolymer comprising vinyl-acetate, -ethers and/or -carbonates,
WO1994029270A1 (en)	1994-12-22	Novel sulfonate, process for producing the same, and bleaching composition containing the same
KR20130038919A (ko)	2013-04-18	모노카복실산과 디카복실산의 공중합체, 그의 제조 및 용도
JPH07505663A (ja)	1995-06-22	重合体および重合体を含有する洗剤組成物
EP0641363B1 (en)	1997-01-08	Detergent compositions containing copolymers
EP0534772A2 (en)	1993-03-31	Oxidising compositions
WO2024126268A1 (en)	2024-06-20	Biodegradable graft polymers for dye transfer inhibition
EP4172297B1 (en)	2024-08-28	Laundry detergent formulation with biodegradable antiredeposition agent
JPH04209644A (ja)	1992-07-31	重合体及びそれを含有する洗剤組成物
JPH0786128B2 (ja)	1995-09-20	ポリカルボキシレート化合物及びそれを含有する洗剤組成物
US5560749A (en)	1996-10-01	Polymeric bleach precursors and methods of bleaching substrates
EP4386020A1 (en)	2024-06-19	Biodegradable graft polymers for dye transfer inhibition